עדיין מחפשים עבודה במנועי חיפוש? הגיע הזמן להשתדרג!
במקום לעבור לבד על אלפי מודעות, Jobify מנתחת את קורות החיים שלך ומציגה לך רק משרות שבאמת מתאימות לך.
מעל 80,000 משרות • 4,000 חדשות ביום
חינם. בלי פרסומות. בלי אותיות קטנות.
מלאה
18,000-25,000 ₪
Join a growing biotech company in the final stages of FDA submission!
Were looking for a hands-on Validation engineer with strong experience in writing and executing validation protocols and reports. This is a key role reporting directly to the Engineering Manager.
Responsibilities:
Write and execute validation protocols (IQ/OQ/PQ)
Prepare comprehensive validation documentation including plans, protocols, reports, deviations, and CAPAs
Collaborate with cross-functional teams: Engineering, QA, RA, and Manufacturing
Support internal and external audits, including FDA readiness
Maintain and improve validation procedures in compliance with GMP, FDA, and ISO standards
Were looking for a hands-on Validation engineer with strong experience in writing and executing validation protocols and reports. This is a key role reporting directly to the Engineering Manager.
Responsibilities:
Write and execute validation protocols (IQ/OQ/PQ)
Prepare comprehensive validation documentation including plans, protocols, reports, deviations, and CAPAs
Collaborate with cross-functional teams: Engineering, QA, RA, and Manufacturing
Support internal and external audits, including FDA readiness
Maintain and improve validation procedures in compliance with GMP, FDA, and ISO standards
Requirements:
B.Sc. in Engineering, Life Sciences, or related field
At least 3 years as Validation engineer
hands-on experience in validation within pharma/biotech industry
Proven experience in writing and executing protocols and validation reports
Solid understanding of regulatory requirements (GMP, FDA, ISO)
Detail-oriented, self-motivated, and capable of managing multiple tasks
High-level English (written and verbal) a must
Advantages:
Experience in startups or companies preparing for FDA submissions
Familiarity with aseptic manufacturing
B.Sc. in Engineering, Life Sciences, or related field
At least 3 years as Validation engineer
hands-on experience in validation within pharma/biotech industry
Proven experience in writing and executing protocols and validation reports
Solid understanding of regulatory requirements (GMP, FDA, ISO)
Detail-oriented, self-motivated, and capable of managing multiple tasks
High-level English (written and verbal) a must
Advantages:
Experience in startups or companies preparing for FDA submissions
Familiarity with aseptic manufacturing
This position is open to all candidates.
במקום לעבור לבד על אלפי מודעות, Jobify מנתחת את קורות החיים שלך ומציגה לך רק משרות שבאמת מתאימות לך.
מעל 80,000 משרות • 4,000 חדשות ביום
חינם. בלי פרסומות. בלי אותיות קטנות.
חיפה
